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7-Methoxy-3a,10b-dimethyl-1,2,3,3aalpha,5aalpha,7,10bbeta,10calpha-octahydro-4H,9H- furo(2,3',4':4,5) naphtho(2,1-c)pyran-4,9-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23660-12-0

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23660-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23660-12-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,6,6 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23660-12:
(7*2)+(6*3)+(5*6)+(4*6)+(3*0)+(2*1)+(1*2)=90
90 % 10 = 0
So 23660-12-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H20O5/c1-16-5-4-6-17(2)13(16)11(21-15(17)19)7-9-10(16)8-12(18)22-14(9)20-3/h7-8,11,13-14H,4-6H2,1-3H3/t11-,13-,14+,16-,17+/m1/s1

23660-12-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name LL-Z 1271α

1.2 Other means of identification

Product number -
Other names 7-methoxy-3a,10b-dimethyl-1,2,3,3a,5a,7,10b,10c-octahydro-5,8-dioxaacephenanthrylene-4,9-dione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:23660-12-0 SDS

23660-12-0Downstream Products

23660-12-0Relevant academic research and scientific papers

Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: Metabolites CJ-14,445, LL-Z1271γ, oidiolactones A, B, C, and D, and nagilactone F

Hanessian, Stephen,Boyer, Nicolas,Reddy, Gone Jayapal,Deschenes-Simard, Benoit

, p. 4640 - 4643 (2009)

An efficient, high-yielding strategy has been developed for the asymmetric total synthesis of seven norditerpenoid dilactones known for their diverse biological properties. The three key steps employed to obtain a tricyclic lactone intermediate involved a

An Efficient Synthesis of the Antifungal Dilactone LL-Z1271α and of other Biologically Active Compounds

Barrero, Alejandro F.,Sanchez, Juan F.,Elmerabet, Jamal

, p. 5251 - 5254 (1995)

The syntheses of the terpenoid antifungal LL-Z1271α and other related compounds were achieved starting from the communic acids.The synthetic approach includes a mercuriation-demercuriation reaction of a γ,δ-unsaturated methyl ester in the presence of O2, giving rise to a lactone ring.

Enantiospecific syntheses of the potent bioactives nagilactone F and the mould metabolite LL-Z1271α an evaluation of their allelopathic potential

Barrero, Alejandro F.,Sanchez, Juan F.,Elmerabet, Jamal,Jimenez-Gonzalez, David,Macias, Francisco A.,Simonet, Ana M.

, p. 7289 - 7304 (2007/10/03)

Improved syntheses are described for nagilactone F and the antibiotic LL-Z1271α, two of the most potent bioactive members of the podolactone family. The allelopathic potential of some members of this podolactone series has been evaluated, with the result

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